| Resume alert | Resumes 51 - 60 of 61 |
Project Engineer
San Juan, Puerto Rico
... Pharmaceutical/ FDA, DEA, GMP regulated industry skills. On-site plant knowledge of Safety, OSHA, and FDA regulations. Expert in performing Process, Packaging and Equipment Validations. Team and independently oriented, Excellent technical, ... - 2013 Feb 20
... Pharmaceutical/ FDA, DEA, GMP regulated industry skills. On-site plant knowledge of Safety, OSHA, and FDA regulations. Expert in performing Process, Packaging and Equipment Validations. Team and independently oriented, Excellent technical, ... - 2013 Feb 20
Project Manager Management
Guaynabo, PR, 00769
... FDA Regulated Industries experience( 9 years in medical devices Industry) Detailed-oriented professional with extensive experience in administrative and supplier quality coordination and project management within private and public sectors including ... - 2013 Feb 18
... FDA Regulated Industries experience( 9 years in medical devices Industry) Detailed-oriented professional with extensive experience in administrative and supplier quality coordination and project management within private and public sectors including ... - 2013 Feb 18
Engineer Six Sigma
Barceloneta, 00, Puerto Rico
... EDUCATION Bachelor of Science in Industrial Engineering University of Puerto Rico, Mayagüez Campus SKILLS • Knowledge of Current Good Manufacturing and Documentation Practices, FDA, DEA, Training Techniques and Curriculum, Lean/Kaizen/Six Sigma/ 5S ... - 2012 Oct 14
... EDUCATION Bachelor of Science in Industrial Engineering University of Puerto Rico, Mayagüez Campus SKILLS • Knowledge of Current Good Manufacturing and Documentation Practices, FDA, DEA, Training Techniques and Curriculum, Lean/Kaizen/Six Sigma/ 5S ... - 2012 Oct 14
Management Project
Caguas, PR, 00725
... Seminars: GMP’S, GLP’S, SPC, IQ-OQ-PQ, ISO, FDA, DEA, Safety, Labor relations, Sexual Harassment, Supervision, Cleaning validation, Computer; Excel, Word, Power Point, Statgraphics, SAP system, Trackwise, GxPharma, Open Lab, SQL* LIMS, Empower, ... - 2012 Oct 03
... Seminars: GMP’S, GLP’S, SPC, IQ-OQ-PQ, ISO, FDA, DEA, Safety, Labor relations, Sexual Harassment, Supervision, Cleaning validation, Computer; Excel, Word, Power Point, Statgraphics, SAP system, Trackwise, GxPharma, Open Lab, SQL* LIMS, Empower, ... - 2012 Oct 03
Project Manager System
Cayey, PR, 00737
Luis F.Santiago Colón PO BOX *** Cayey, P.R.***37 787-***-**** Cell: 787-***-**** Email: p2v0bw@r.postjobfree.com Professional Profile IT professional with over 20 years of experience in Electronic industry, Medical devices (FDA Regulated), and ... - 2012 Jun 27
Luis F.Santiago Colón PO BOX *** Cayey, P.R.***37 787-***-**** Cell: 787-***-**** Email: p2v0bw@r.postjobfree.com Professional Profile IT professional with over 20 years of experience in Electronic industry, Medical devices (FDA Regulated), and ... - 2012 Jun 27
Manager Management
Coamo, PR, 00769
... • Compliance with policies and procedures defined by GMP’s, SOP’s, FDA, OSHA regulations and ISO 9000/14000. • Fully Bilingual/ English and Spanish. Professional Experience MATERIALS, PLANNING AND STRATEGIC MANAGER (May 10, 2010 to November 30, 2011 ... - 2012 Feb 14
... • Compliance with policies and procedures defined by GMP’s, SOP’s, FDA, OSHA regulations and ISO 9000/14000. • Fully Bilingual/ English and Spanish. Professional Experience MATERIALS, PLANNING AND STRATEGIC MANAGER (May 10, 2010 to November 30, 2011 ... - 2012 Feb 14
Sr. IT Business System Analyst
Carolina, PR, 00983
... Business Excellence Consulting, Caguas PR, Human Error and Human Factor in FDA Regulated Industry. Business Excellence Consulting, Project Management Methodology. Universidad Politecnica de Puerto Rico. - 2011 Aug 31
... Business Excellence Consulting, Caguas PR, Human Error and Human Factor in FDA Regulated Industry. Business Excellence Consulting, Project Management Methodology. Universidad Politecnica de Puerto Rico. - 2011 Aug 31
Bilingual Manufacturing supervisor
Vega Alta, PR, 00692
... Responsible for productivity and quality line production in Clean Room and Packing, compliance all FDA regulations. Coordinate product shipping to Gamma and ETO. Trained and certificated of manufacturing associates in ISO 9000 and QSR Application. ... - 2009 Nov 07
... Responsible for productivity and quality line production in Clean Room and Packing, compliance all FDA regulations. Coordinate product shipping to Gamma and ETO. Trained and certificated of manufacturing associates in ISO 9000 and QSR Application. ... - 2009 Nov 07
Mechanical Engineer
Ciales, PR, 00638
... - Successfully managed sensitive computer system validation projects until completion of an FDA audit and the subsequent approval of the validation package. - Successfully lead projects in Chicago, Japan and Switzerland developing validation ... - 2009 Aug 29
... - Successfully managed sensitive computer system validation projects until completion of an FDA audit and the subsequent approval of the validation package. - Successfully lead projects in Chicago, Japan and Switzerland developing validation ... - 2009 Aug 29
Electrical Engineer
PR, 00693
... in the pharmaceutical industry with knowledge of Power Systems Design, PLC and HMI programming, Equipment Automation, Control Systems Design and Implementation, Project Management, Capital Appropriation Development, Compliance & FDA requirements. ... - 2009 Aug 03
... in the pharmaceutical industry with knowledge of Power Systems Design, PLC and HMI programming, Equipment Automation, Control Systems Design and Implementation, Project Management, Capital Appropriation Development, Compliance & FDA requirements. ... - 2009 Aug 03